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Guidance on the planning for mineral extraction in plan making and the application process.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
How to use an interrupted time series to evaluate your digital health product.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Explains how victims of persistent antisocial behaviour have the right to request a case review where a local threshold is met.
Tips at work do not count towards the National Minimum Wage - tips and tax, what your employer has to do, advice and help, cash in hand payments
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Watch our caseworkers' top tips to make sure your applications are complete and correct. Avoid more than 20 common requisition points.
A summary of what attending a review panel is like and the documents that you can submit to the Independent Review Mechanism (IRM).
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How health app content should be reviewed by subject matter experts.
How test manufacturers or distributors can apply for approval of their tests to sell on the UK market.
How to apply for simultaneous review of veterinary medicine submissions to the Australian Pesticides and Veterinary Medicines Authority (APVMA) and the VMD.
Guidance to government departments on the RPC's scrutiny process.
Using an ecological momentary assessment to evaluate your digital health product.
Find out what we will check, the records you need to keep and how we treat breaches in the ISA rules.
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